Average salary: £50,000 /yearly
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Senior Regulatory Affairs Manager CMC
A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs... ...development, execution and tracking of regulatory CMC and medical device activities. Candidates must have protein experience in addition...
Medical device
...Regulatory Affairs Specialist - Fully Remote This is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing... ...& SaMD - as well as proven experience working with medical devices that use AI & Machine Learning. The purpose of this...
Medical device
Work at office
Immediate start
Remote job
Holiday work
£39k - £52k per annumEstimated
...Origin Sciences is a start-up biotechnology company based in Granta Park, just south of Cambridge. We develop our own innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank provides clinical material for our...
Medical device
Full time
Hybrid work
Holiday work
...Instrumentation - Cambridge
A growing Medical Devices Division is currently seeking an... ...companies.
Newton Colmore Consulting is a specialist recruitment company within the Medical... ...Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field...
Medical device
Medical Devices - Senior Mechanical Design Engineer - Cambridge
Due to successful growth plans... ...physicists, and other Medical Devices specialists, you will tackle some of the most... ...Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field Service...
Medical device
Medical Devices Mechanical Engineer - SolidWorks - Cambridge
A growing Medical Devices group... ...Recruitment and Scientific Recruitment Specialist at Newton Colmore, on (***) ***-****,... ..., New Product Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field Service...
Medical device
...risk missing out.
Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Scientific Software,... ...Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering...
Medical device
Validation Engineer - Medical Devices
A growing medical devices company based in Cambridgeshire... ...activities required ahead of regulatory approval, product launch, and mass manufacturing... ...and much more.
Newton Colmore is a specialist executive search and talent solutions...
Medical device
Holiday work
Regulatory Affairs and Quality Assurance Assistant - Medical Devices - Cambridge
Due to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company's Quality Assurance...
Medical device
Immediate start
...Medical Devices Consultant - Senior Mechanical Engineer - Cambridge
Due to the growth of a... ...Recruitment and Scientific Recruitment Specialist at Newton Colmore, at (***) ***-****.... ...Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field...
Medical device
Senior Verification Engineer - Medical Devices
Newton Colmore is working with an up-and-coming... ....
Ensure the adherence to ISO 13485 regulatory standards.
The implementation of the... ...and much more.
Newton Colmore is a specialist executive search and talent solutions...
Medical device
Holiday work
Senior Manager Regulatory Affairs Writing
A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory... ...agencies.
scientific contribution to the development of medical, regulatory and clinical documents to support development...
Suggested
Contract work
...departments)
Advanced command of written and spoken English,
Preferably regulatory work experience in a pharmaceutical company:
Min 1 year of Regulatory Affairs experience for Specialist position
Min 4 years of Regulatory Affairs experience for Executive position...
Suggested
Work at office
Local area
Human Factors Design Engineer - Medical Devices - Cambridge
A Medical Devices company, based in Cambridgeshire, is currently looking for a Human Factors Design Engineer to assist with the ongoing development of new Medical Devices.
Working alongside an established R&D...
Medical device
Medical Devices Electronics Engineer - Circuits Design - Embedded Software - Cambridge
A growing Medical Devices company, based in Cambridge, is currently looking for an experienced Electronics Engineer to assist with the circuit design of a range of brand-new Medical Devices...
Medical device
Global Regulatory and Operations Senior Director page is loaded Global Regulatory and Operations Senior Director
Apply locations GB Cambridge... ...Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory...
Permanent employment
Full time
Work at office
Local area
Hybrid work
Flexible hours
£37k - £48k per annumEstimated
...Cambridge Design Partnership are looking for Specialist Mechanical Engineers with significant expertise and experience in developing medical devices to join our network of approved... ...the various needs from the medical device regulatory requirements such as IEC 60601 ISO 1348...
Medical device
For contractors
...Medical Devices - Senior Mechanical Design Engineer - Cambridge
Due to successful growth... ...physicists, and other Medical Devices specialists, you will tackle some of the most complex... ...Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field...
Medical device
...healthcare professionals, our partners, and our employees.
Ensure continuous compliance of Mundipharma RA operations across diverse regulatory landscapes in the EU and Canada.
# Drive RA operations to meet business requirements while adhering to budgetary constraints.
#...
Permanent employment
Work at office
Local area
Hybrid work
Flexible hours
...Job Purpose
The Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead the development... ...Regulatory writing activities
Partners with Regulatory Affairs and cross-functional colleagues to understand the clinical...
Permanent employment
Contract work
Work at office
Remote job
Hybrid work
Flexible hours
2 days week
